Cas 139331-06-9,3-Benzyl-2-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ<sup>6</sup>-thia-4-aza-tricyclo[5.2.1.0<sup>1,5</sup>]decane-4-carbonyl)-6-isopropoxy-[1,2,5]oxadiazinan-4-one

139331-06-9

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Basic information

Product Name: 3-Benzyl-2-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-6-isopropoxy-[1,2,5]oxadiazinan-4-one
Synonyms:
CAS NO:139331-06-9
Molecular Formula:
Molecular Weight: 491.609
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-Benzyl-2-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-6-isopropoxy-[1,2,5]oxadiazinan-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-Benzyl-2-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-6-isopropoxy-[1,2,5]oxadiazinan-4-one(139331-06-9)
EPA Substance Registry System: 3-Benzyl-2-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-6-isopropoxy-[1,2,5]oxadiazinan-4-one(139331-06-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 139331-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139331-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,3 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139331-06:
(8*1)+(7*3)+(6*9)+(5*3)+(4*3)+(3*1)+(2*0)+(1*6)=119
119 % 10 = 9
So 139331-06-9 is a valid CAS Registry Number.

139331-06-9Upstream product

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139331-06-9Relevant academic research and scientific papers

Asymmetric Diels-Alder reactions of a nitroso compound derived from D-bornane-10,2-sultam

Gouverneur,Dive,Ghosez

, p. 1173 - 1176 (1991)

Acylnitroso dienophile 3 derived from D-bornane-10,2-sultam undergoes cycloaddition with high yields and complete facial selectivity to cyclopentadiene and cyclohexadiene. When the nitroso group is attached to the sultam nitrogen, it is no longer reactive

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